FdaApprovalPulse: records in Tennessee
8 fdaApprovalPulse: records in Tennessee are listed from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-06-05 to 2026-08-26; the most frequent is Medtronic Sofamor Danek USA, Inc. with 4. Data last updated 2026-11-04; each record links to its official source and a full report.
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Includes: Sponsor, Product, Approval, Decided, official source URL and score · Card, Apple Pay, Google Pay or Link via Stripe
8 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), dated 2026-06-05 to 2026-08-26. Most frequent: Medtronic Sofamor Danek USA, Inc. (4). Each record links to a full report and the official source.
Last updated 2026-11-04. Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
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- Medtronic Sofamor Danek USA, Inc. (4)
- Medtronic, Inc. (2)
- Cyndrx, LLC (1)
- Lynch Biologics, LLC (1)
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What are the top fdaApprovalPulse: records in Tennessee right now?
| Record | Product | Approval | Decided |
|---|---|---|---|
| Cyndrx, LLC | AbsorbaSeal 5.6.7F Vascular Closure Device | PMA original approval (new class III device) | 2026-06-05 |
| Medtronic Sofamor Danek USA, Inc. | INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE | PMA supplement (device change) | 2026-08-26 |
| Medtronic Sofamor Danek USA, Inc. | INFUSE BONE GRAFT | PMA supplement (device change) | 2026-08-26 |
| Medtronic, Inc. | INFUSE BONE GRAFT | PMA supplement (device change) | 2026-08-26 |
| Lynch Biologics, LLC | GEM21S® Growth Factor Enhanced Matrix Implementation of Restricted Access Barrier System (RABS) at Pyramid | PMA supplement (device change) | 2026-08-03 |
| Medtronic, Inc. | Infuse Bone Graft | PMA supplement (device change) | 2026-07-28 |
| Medtronic Sofamor Danek USA, Inc. | Infuse Bone Graft | PMA supplement (device change) | 2026-07-28 |
| Medtronic Sofamor Danek USA, Inc. | Infuse TM Bone Graft/Medtronic lnterbody Fusion Device | PMA supplement (device change) | 2026-07-28 |
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Drug labeling or REMS supplement (1180) PMA supplement (device change) (367) Generic drug approval (ANDA) (196) Drug efficacy supplement (new indication or use) (77) Drug manufacturing (CMC) supplement (55) New drug application (NDA) (41) PMA original approval (new class III device) (24) Biologic license (BLA) (17) Other drug supplement (12)
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Frequently asked questions
How many fdaApprovalPulse: records in Tennessee are listed?
8 records from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration), last refreshed automatically. The most recent is dated 2026-08-26.
Can I get alerts for Tennessee?
Yes. FdaApprovalPulse can email you new records matching this filter; plans are listed on the FdaApprovalPulse page.
Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration). Informational only. RSS feed of new records